Dermatopolymyositis

dermatomyositis: Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness.

Endpoint definition

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FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 M33
Cause of death: ICD-10 M33

Check pre-conditions None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_DERMATOPOLY

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M30-M36
Name in latin Dermato[poly]myositis

Summary Statistics

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Key figures

All Female Male
Number of individuals 262 170 92
Unadjusted prevalence (%) 0.10 0.12 0.08
Mean age at first event (years) 50.95 50.46 51.86

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 0.02 1.04 [0.23, 4.61] 9.6e-1 45
15 years 0.01 1.56 [0.44, 5.59] 4.9e-1 38
5 years 0.00 3.18 [1.18, 8.61] 2.3e-2 18
1 year - - - -

Correlations

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Index endpoint: M13_DERMATOPOLY – Dermatopolymyositis
GWS hits: 0

Survival analyses between endpoints

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Plot

before Dermatopolymyositis
after Dermatopolymyositis

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Dermatopolymyositis

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